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exo-1-bromo-4,4-dimethyl-3,5,8-trioxatricyclo[5.2.2.0]undec-10-en-9-one | 134593-84-3

中文名称
——
中文别名
——
英文名称
exo-1-bromo-4,4-dimethyl-3,5,8-trioxatricyclo[5.2.2.0]undec-10-en-9-one
英文别名
(1R,2R,6R,7R)-1-bromo-4,4-dimethyl-3,5,8-trioxatricyclo[5.2.2.02,6]undec-10-en-9-one
exo-1-bromo-4,4-dimethyl-3,5,8-trioxatricyclo[5.2.2.0]undec-10-en-9-one化学式
CAS
134593-84-3;134678-33-4
化学式
C10H11BrO4
mdl
——
分子量
275.099
InChiKey
VAQBXQZTEAHEFD-DAGMQNCNSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.14
  • 重原子数:
    15.0
  • 可旋转键数:
    0.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    44.76
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

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文献信息

  • Modified Nucleosides for Rna Interference
    申请人:Herdewijn Piet
    公开号:US20080261905A1
    公开(公告)日:2008-10-23
    The present invention relates to the use of modified nucleotides and single or double stranded oligonucleotides having at least one of said modified nucleotides for performing RNA interference. The modified nucleotides are selected from 6-membered ring containing nucleotides such as hexitol, altritol, O-substituted or O-alkylated altritol, cyclohexenyl, ribo-cyclohexenyl and O-substituted or O-alkylated ribo-cyclohexenyl nucleotides. The present invention also relates to novel modified nucleosides or nucleotides and to the use of the novel modified nucleosides and nucleotides in single or double stranded oligonucleotides for RNA interference, antisense therapy or other applications.
    本发明涉及使用修饰核苷酸和至少含有其中一种修饰核苷酸的单链或双链寡核苷酸来进行RNA干扰。修饰核苷酸从包含六元环的核苷酸中选择,例如己糖醇,阿尔特糖醇,O-取代或O-烷基化的阿尔特糖醇,环己烯基,核糖-环己烯基和O-取代或O-烷基化的核糖-环己烯基核苷酸。本发明还涉及新型修饰核苷或核苷酸以及在单链或双链寡核苷酸中使用新型修饰核苷和核苷酸进行RNA干扰、反义治疗或其他应用。
  • 3-bromo-2-pyrone: an easily prepared chameleon diene and a synthetic equivalent of 2-pyrone in thermal diels-alder cycloadditions
    作者:Gary H. Posner、Todd D. Nelson、Chris M. Kinter、Kamyar Afarinkia
    DOI:10.1016/s0040-4039(00)92368-2
    日期:1991.9
    3-Bromo-2-pyrone, a stable solid prepared by a new route (eq. 1), has been found to undergo smooth and regiospecific 2+4-cycloadditions between 78-90-degrees-C with both electron-rich and electron-deficient dienophiles; subsequent high-yield reductive debrominations produced halogen-free cycloadducts thus showing 3-bromo-2-pyrone to be a practical and effective synthetic equivalent of 2-pyrone in thermal Diels-Alder cycloadditions.
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